Chem Lecture Test 1 IPT
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Lecture Test...
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Chem Lecture T1 15 JD TY N Memory Work What to memorise Isotopes
Ionisation energy
Metallic Bonding Ionic Bonding Covalent Bonds Explaining why dative bonds form
Polarity
Definition Have same proton number but different nucleon number Same chemical properties, but different physics properties Atoms of an element First Ionisation energy is the amount of energy required to remove 1 mole of electrons from 1 mole of gaseous atoms to form 1 mole of unipositive gaseous ions. Second ionisation energy is the amount of energy required to remove 1 mole of electrons from 1 mole of unipositive gaseous ions to form 1 mole of gaseous ions with double positive charge. Electrostatic force of attraction between metal cations and sea of delocalised electrons Electrostatic force of attraction between oppositely charged ions Electrostatic force of attraction between nucleus of the two bonded atoms ahd shared pair of electrons Because one of the molecular has lone pairs and can act as an electron donor while the other molecular has only 1/2/3 electron pairs, has an empty orbital in valence shell and can accept the donated electrons to achieve octet. Separation of Charge, unequal sharing of charge, dipole moments
Explaining solubility/interaction between ionic and covalent substances Theory Substantiation Covalent Covalent Energy released from Solute solvent Need to IDENTIFY the different types of interaction greater than/smaller than interaction in solute solute, solvent solvent, energy required to break solute solute and solute solvent before elaborating. solvent solvent bonds
Chem Lecture T1 15 JD TY N
Then proceed to explain which bond is the stronger one and how it leads to the solubility.
Ionic Compounds Need to IDENTIFY the different types of Energy released from ion-‐dipole interaction in solute solute, solvent solvent, interactions >/< energy needed to break solute solvent before elaborating. hydrogen bonds of water and solute solute bonds, detaches ion from surface Then proceed to explain which bond is the stronger one and how it leads to the solubility.
Sketching Important Trends
Trend Atomic Radius Across the Period
Sketch+Explain
1. Atomic radius decreases down the period as -‐ Nuclear charge increases due to increasing proton number -‐ Shielding effect remains relatively constant -‐ Effective Nuclear Charge increases -‐ Electrostatic forces of attraction between ____ and _____ increases
Chem Lecture T1 15 JD TY N -‐ More energy required to overcome
2. Ionic radius generally decreases down the period, except for huge jump from cations to anions -‐ Nuclear charge increases -‐ Shielding effect remains relatively constant -‐ Effective Nuclear Charge increases -‐ Electrostatic forces of attraction between ____ and _____ increases -‐ Sharp jump from cations to anions due to additional quantum shell of electrons (3s and 3p)
3. Trends in successive I.E -‐ Small increases when moving from p orbital to s as s orbitals at higher energy level as they are CLOSER to the nucleus -‐ Large jump when next electron is removed from an inner quantum shell (look at the number of valence electrons)
Chem Lecture T1 15 JD TY N
4. Trends in IE across period -‐ Nuclear charge increases across period -‐ Shielding effect remains relatively constant -‐ ENC increases -‐ Electrostatic forces of attraction between ___ and ___ increases -‐ More energy needed to remove outermost electron Some anomalies -‐ Small dip from Mg to Al as 3p subshell of al at higher energy level than 3s of Mg, weaker attraction between nucleus and outermost electron, less energy required. -‐ Inter-‐electronic repulsion for paired electrons in 3p subshell of S, less energy required to remove the more unstable electrons.
Deducing strength of Bonds Type of bond Metallic
Ionic
Covalent
Explanation -‐Compare number of valence electrons contributed PER METAL ATOM (Stronger/weaker electrostatic forces of attraction) -‐Charge, radius and charge density. Larger the charge and smaller the radius, ,the stronger the bond. Lattice Energy (Charge of cation, anion, radius of cation, anion) Remember to break cations and anions up separately to compare and analyze. Polarity, size and number of bonds (The smaller the atom, the more effective the orbital overlap, the closer to the nucleus.
Chem Lecture T1 15 JD TY N The more polar, the shorter the bond length. The more number of bonds, the stronger the attraction between nucleus and shared electrons.) Explaining Chemical/Physical Properties Type Properties Metals 1. High Melting and Boiling Points -‐ Exist as giant metallic lattice, strong electrostatic forces of attraction between metal cations and sea of delocalised electrons, more energy needed to break.. 2. Good electrical conductivity -‐ Sea of delocalised electrons to act as mobile charge carriers 3. Good heat conductors -‐ Heat energy picked up by electrons to vibrate faster (kinetic energy) 4. Shiny surface -‐ When photon strike surface, osicillating electric field causes electrons on surface to oscillate. Photon bounces off without loss of momentum. 5. Hardness -‐ Strong metallic bond 6. Malleable and ductile -‐ Layers of ions can slide over one another into new position. Sea of delocalised electrons reduces repulsions between cations, so do not break. 7. Alloy -‐ Disrupt orderly arrangement of metal atoms Ionic Compounds 1. High Melting and Boiling Points -‐ Exist as giant metallic lattice, strong electrostatic forces of attraction between metal cations and sea of delocalised electrons, more energy needed to break..
Chem Lecture T1 15 JD TY N
Covalent
2. Good Electrical conductors in molten/aqueous state -‐ Ions in solid state are held in a fixed lattice, but when dissociated can act as mobile charge carriers 3. Hard, rigid but brittle -‐ Hard force may cause ions of like charges to become next to each other, causing repulsion and lattice to shatter. 1. Low melting and boiling point for simple molecular structures and high for Giant covalent structures -‐ SMS molecules held by weak VDW forces -‐ GCS molecules held by strong covalent bonds 2. Most do not conduct electricity except for Graphite -‐ As electrons are held in covalent bonds/nucleus -‐ As for graphite, each carbon is only covalently bonded to three others, there is a spare electron to act as mobile charge carrier Drawing Sigma/PI bonds
Type Drawing of Bond Sigm a Bond
Chem Lecture T1 15 JD TY N Pi Bond
1s, 2s, 3s
Note: 2s orbital larger than 1s, 3s larger than 2s Explaining difference between bond angles Theory Explanation 1. Compare number of electron pairs If electron pairs is different, then first immediately use VSEPR to explain 2. Compare number of lone pairs if Lone pair lone pair repulsion is the electron pairs is the same strongest, so it will push bond pairs closer. 3. If all are the same, use polarity. A more polar molecular will have Remember the sequence= LP-‐LP slightly differing bond angles than a repulsion> LP-‐BP Repulsion > BP-‐BP less polar one. repulsion. Electrons in a more polar molecule will be attracted to __, leading to decrease in BP-‐BP repulsion (depends) and increase in LP-‐BP repulsion.
Determining Difference Between Melting/Boiling Points
Key
Possible ways of Answering Required
Chem Lecture T1 15 JD TY N Remember that melting/boiling points are always due to intermolecular forces of attraction. Ionic compounds: Ions Metallic compounds: Ions and Delocalised electrons Covalent compounds: Molecules
Check for Differences in type of bonding 1. Comparing the structure (Ionic VS Covalent VS metallic compounds) -‐ Giant ionic lattice, simple molecular structure, giant molecular structure, giant metallic lattice Check for Hydrogen Bonds
2. Hydrogen bonds are strong -‐ Requires FON with lone pair -‐ H bonded to FON Confirm the Intermolecular Force 3. Polar or Non-‐Polar -‐ Non-‐polar compounds have dispersion forces, which are weaker than the permanent dipole permanent dipole interactions in polar compounds Non Polar Compounds Check for difference in Mr 4. If both molecules are non-‐ polar, compare Mr -‐ Larger Mr means larger electron cloud, more polarisable, more formation of induced and instantaneous dipoles, stronger dispersion forces Check for Branches 5. If both molecules are non-‐ polar, compare the surface area -‐ A straight chain compound has larger points of comtact that
Chem Lecture T1 15 JD TY N dispersion forces can act. Therefore, stronger dispersion forces.
Polar Compounds Difference in Polarity 6. Increase in polarity leads to shorter bond length -‐ More polar means shorter bond length, electron more attracted to nucleus, more energy needed to break bonds
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